Tůma S, Hucín B, Reich O, Vorísková M, Radvanský J
Pediatrické kardiocentrum, Fakultní nemocnice s poliklinikou v Motole, Praha.
Cesk Pediatr. 1990 Sep;45(9):543-5.
A rare case of the abnormal origin of the right coronary artery is demonstrated in a two-year-old boy with an aortopulmonary window and subvalvular membranous aortal stenosis. The diagnosis was established by angiography before operation by injection of contrast substance into both great arteries. Surgical repair of the complicated defect comprised also derivation of the orifice of the right coronary artery into the aorta. The long-term postoperative follow-up indicates relatively favourable results with signs of impaired myocardial perfusion in the area supplied by the right coronary artery.
一名患有主肺动脉窗和主动脉瓣下膜性狭窄的两岁男孩,显示出右冠状动脉异常起源的罕见病例。术前通过向两根大动脉注射造影剂进行血管造影确诊。复杂缺损的手术修复还包括将右冠状动脉口转位至主动脉。术后长期随访显示结果相对良好,但右冠状动脉供血区域有心肌灌注受损的迹象。